Researchers developed an innovative vaccine strategy that uses genetically modified viruses to protect against Chikungunya and other diseases. The new approach generates antibodies without causing disease, paving the way for a robust vaccine platform with broad protective potential.
SourceFundação de Amparo à Pesquisa do Estado de São Paulo·Journalnpj Vaccines·DateAug 5, 2026
JMIR Publications invites submissions on the 2026 Ebola disease public health emergency of international concern, focusing on response strategies, risk communication, and surveillance. The World Health Organization has declared a public health emergency due to population mobility and ongoing uncertainty in the Democratic Republic of th...
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Researchers from The University of Osaka developed a new technique using mass photometry to detect and quantify components of rAAV particles. This method can distinguish between full and empty particles, streamlining gene therapy manufacturing and improving clinical effectiveness.
SourceThe University of Osaka·JournalAnalytical Chemistry·TypeExperimental study·DateMay 12, 2025
Researchers at Tel Aviv University discovered a variant of TMEM16F protein that enhances the spread of Parkinson's pathology, potentially leading to new treatments. The study found that cells with the mutation secrete more pathological α-synuclein, which can form Lewy bodies and damage brain cells.
Researchers developed a compact 'gene scissor' tool, TnpB, which shows a 4.4-fold increase in efficiency of modifying DNA, making it more effective as a gene editing tool. The tool can be used to treat patients with familial hypercholesterolemia, reducing cholesterol levels by nearly 80%.
SourceUniversity of Zurich·JournalNature Methods·TypeExperimental study·DateSep 23, 2024
In a mouse model of multiple system atrophy, alpha-synuclein overexpression induces neuroinflammation, demyelination, and neurodegeneration. IFNγ produced by infiltrating CD4+ T-cells mediates these changes. The study suggests that IFNγ is a potential future disease-modifying therapeutic target.
SourceUniversity of Alabama at Birmingham·JournalActa Neuropathologica Communications·TypeExperimental study·DateFeb 12, 2024
Researchers have developed an oncolytic virus that can 'warm up' cold tumors and improve immunotherapy outcomes. The virus was engineered to carry a gene encoding a TGF-β inhibitor, which greatly increased survival rates in mice with aggressive melanoma and other cancers.
SourceUniversity of Pittsburgh·JournalJournal of Experimental Medicine·TypeExperimental study·DateAug 14, 2023
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Researchers from IMBA identify a family of virus-like transposons called Mavericks that facilitate horizontal gene transfer (HGT) between reproductively isolated worm species. The study reveals the role of Mavericks in overcoming the species barrier, with potential applications in pathogen control and genomic innovation.
SourceIMBA- Institute of Molecular Biotechnology of the Austrian Academy of Sciences·JournalScience·TypeExperimental study·DateJun 29, 2023
Researchers found that combining radiation with a genetically engineered oncolytic vaccinia virus improved treatment outcomes for glioblastoma brain tumors in mice. The combination showed a 15% cure rate and 62% rejection of new cancer cells, outperforming radiation alone.
SourceUniversity of Alberta·JournalCancer Letters·TypeExperimental study·DateJun 20, 2023
A Dartmouth study reveals that disruptions in the mTORC1 pathway can rescue neuronal overgrowth and synapse function dysregulated by Pten loss, potentially offering new treatments for autism spectrum disorders. The research team also found that administering Rapamycin to children showed some benefit to symptoms of autism.
SourceThe Geisel School of Medicine at Dartmouth·JournalCell Reports·TypeExperimental study·DateNov 1, 2022
Researchers at the University of Bologna have developed a new targeted cancer therapy based on a genetically modified phage that selectively eliminates tumour cells. The virus is engineered to transport a drug activated by light to target tumour cells, reducing side effects.
SourceUniversità di Bologna·JournalNanoscale·DateMar 10, 2022
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Researchers are exploring how an engineered adeno-associated virus (AAV) can compensate for missing protein or swap out genetic mutations that cause vision problems. AAV has been found to be beneficial and is being used as a tool to deliver genes that work as they should.
Isaac Hilton is using non-integrating episomal DNA viruses to create a new platform technology for cell and gene therapies. He aims to hijack these viruses to safely program medicinal functions in human cells.
Scientists have engineered mosquitoes that can't spread all four types of the dengue virus, a major breakthrough in controlling the disease. This development has the potential to limit human suffering and mortality from dengue, which affects over 390 million people annually.
SourceCSIRO Australia·JournalPLOS Pathogens·DateJan 16, 2020
A US defense agency program aims to genetically modify crops using infectious viruses, sparking concerns about its potential military applications and the risk of creating new biological weapons. The approach, known as HEGAAs, would deliver the viruses through insects, raising questions about transparency and public deliberation.
SourceAmerican Association for the Advancement of Science (AAAS)·JournalScience·DateOct 4, 2018
Researchers genetically engineered a Zika virus infectious cDNA clone, enabling rapid vaccine development and exploration of the virus's evolution and transmission. The study unlocks insights into why the Zika virus causes severe diseases and epidemics.
SourceUniversity of Texas Medical Branch at Galveston·JournalCell Host & Microbe·DateMay 16, 2016
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Researchers at MIT have found a way to add genetically modified viruses to the production of nanowires, which can serve as one of a battery's electrodes. This increases the surface area, allowing for more efficient charging and discharging.
SourceMassachusetts Institute of Technology·JournalNature Communications·DateNov 13, 2013
Princeton University researchers are developing a new method for studying brain connectivity using genetically engineered viruses. The viruses, designed by Lynn Enquist's team, travel through the nervous system, tracing connections between neurons and reporting on their activity. This approach has significant implications for understan...
Researchers discovered a genetically engineered herpes simplex virus reduces smooth muscle cell proliferation and restores endothelial layer in arteries following angioplasty. This study provides an important step towards treating vascular disease with genetically engineered viruses.
SourceUniversity of Chicago Medical Center·JournalProceedings of the National Academy of Sciences·DateJul 10, 2007
Researchers at the University of Rochester and UCLA have discovered a novel way to target HIV by genetically engineering a mutant tRNA primer that disrupts the virus's replication process. The approach, which has been patented, opens up new avenues for gene therapy in AIDS treatment.
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